Active — Not RecruitingNot Applicable

DBT Skills Groups for Veterans at High Risk for Suicide Attempt

United States156 participantsStarted 2023-04-30

Plain-language summary

Veteran suicide death is a national crisis. Risk factors include emotion dysregulation, which occurs across mental health disorders. Dialectical behavior therapy (DBT) is an evidence-based suicide intervention that targets emotion dysregulation but is resource-intensive and not widely available at VHA. A more efficient evidence-based DBT Skills Group (DBT-SG) is associated with reduced suicidal ideation and emotion dysregulation and likely more feasible to implement at VHA. This is a randomized controlled trial to test whether DBT-SG in addition to VHA treatment-as-usual, compared to only VHA treatment-as-usual, reduces Veteran emotion dysregulation.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Veteran eligible for VHA care at participating site * two or more suicide attempts in lifetime, with one in past 12 months, on Columbia-Suicide Severity Rating Scale (C-SSRS) * current suicidal ideation (endorsing a suicidal ideation scale of at least 1 \[passive ideation\] on C-SSRS * emotion dysregulation (score 95 or greater on DERS) * can attend group sessions * willing to provide contact information for at least one person who can help locate the participant if study staff are unable to contact them (information for three contact persons will be requested; a participant must provide at least one contact person's information to be included in the study) * access to telephone; if insufficient access to videoteleconference and local facility is using remote procedures for study, willing to request access to VA-provided device Exclusion Criteria: * significant cognitive impairment (score \< 28 on modified Telephone Interview for Cognitive Status (mTICS) * inability to read English or communicate in spoken and written English * plan to move away or be unavailable in the next 18 months

What they're measuring

Change in Emotion dysregulation

Timeframe: Up to18 month follow-up

Trial details

NCT IDNCT05000749

SponsorVA Office of Research and Development

Sponsor typeFED

Study typeINTERVENTIONAL

Primary completion2027-02-26